Canonical Allele Identifier: CA1803689145

Gene: INTS8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827785G= , CM000670.2:g.94827785G=	GRCh38
NC_000008.10:g.95840013G= , CM000670.1:g.95840013G=	GRCh37
NC_000008.9:g.95909189G=	NCBI36
NG_047163.1:g.19475G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.510G= MANE Select	ENSP00000430338.1:p.Gln170=
ENST00000343161.8:c.510G=	ENSP00000343274.4:p.Gln170=
ENST00000519053.5:c.183G=	ENSP00000429056.1:p.Gln61=
ENST00000519457.5:c.369G=	ENSP00000428260.1:p.Gln123=
ENST00000521860.5:c.472G=
ENST00000522171.5:c.387G=	ENSP00000429340.1:p.Gln129=
ENST00000523206.5:c.510G=	ENSP00000429452.1:p.Gln170=
ENST00000523321.5:n.635G=
ENST00000523731.5:c.510G=	ENSP00000430338.1:p.Gln170=
ENST00000524333.5:c.510G=	ENSP00000427840.1:p.Gln170=
NM_017864.3:c.510G=	NP_060334.2:p.Gln170=
NR_073444.1:n.652G=
NR_073445.1:n.652G=
XM_006716602.2:c.510G=	XP_006716665.1:p.Gln170=
XM_006716603.2:c.183G=	XP_006716666.1:p.Gln61=
XM_011517155.1:c.387G=	XP_011515457.1:p.Gln129=
XM_011517156.1:c.510G=	XP_011515458.1:p.Gln170=
XM_011517157.1:c.183G=	XP_011515459.1:p.Gln61=
XM_017013616.1:c.510G=	XP_016869105.1:p.Gln170=
XM_017013617.1:c.510G=	XP_016869106.1:p.Gln170=
XM_017013618.1:c.183G=	XP_016869107.1:p.Gln61=
XM_017013619.1:c.-774G=	XP_016869108.1:n.-774G=
NM_017864.4:c.510G= MANE Select	NP_060334.2:p.Gln170=
NR_073444.2:n.655G=
NR_073445.2:n.655G=